Canonical Allele Identifier: CA328041573
Gene: CYBB HGNC NCBI

Linked Data

dbSNP Id: rs954176527
gnomAD v4: X-37803810-A-G
MyVariant Identifiers: chrX:g.37803810A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37803810A>G , CM000685.2:g.37803810A>G GRCh38
NC_000023.10:g.37663063A>G , CM000685.1:g.37663063A>G GRCh37
NC_000023.9:g.37548007A>G NCBI36
NG_009065.1:g.28794A>G , LRG_53:g.28794A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696170.1:c.*407-67A>G ENSP00000512461.1:n.*407-67A>G
ENST00000696171.1:c.802-67A>G ENSP00000512462.1:n.802-67A>G
ENST00000378588.5:c.898-67A>G MANE Select ENSP00000367851.4:n.898-67A>G
ENST00000378588.4:c.898-67A>G ENSP00000367851.4:n.898-67A>G
ENST00000465127.1:c.171+377810A>G ENSP00000417050.1:n.171+377810A>G
ENST00000492288.1:n.323-67A>G
NM_000397.3:c.898-67A>G , LRG_53t1:c.898-67A>G NP_000388.2:n.898-67A>G
XM_011543890.1:c.592-67A>G XP_011542192.1:n.592-67A>G
NM_000397.4:c.898-67A>G MANE Select NP_000388.2:n.898-67A>G